ENST00000295897.9:c.1437G>A
MANE Select
|
ENSP00000295897.4:p.Val479=
|
|
ENST00000295897.8:c.1437G>A
|
ENSP00000295897.4:p.Val479=
|
|
ENST00000401494.7:c.1092G>A
|
ENSP00000384695.3:p.Val364=
|
|
ENST00000415165.6:c.861G>A
|
ENSP00000401820.2:p.Val287=
|
|
ENST00000476441.6:c.*716G>A
|
ENSP00000423727.1:n.*716G>A
|
|
ENST00000486939.1:n.91G>A
|
|
|
ENST00000503124.5:c.987G>A
|
ENSP00000421027.1:p.Val329=
|
|
ENST00000505649.5:n.984G>A
|
|
|
ENST00000509063.5:c.1437G>A
|
ENSP00000422784.1:p.Val479=
|
|
ENST00000511370.1:c.970G>A
|
|
|
ENST00000621085.4:c.798G>A
|
ENSP00000483421.1:p.Val266=
|
|
ENST00000621628.4:c.798G>A
|
ENSP00000480485.1:p.Val266=
|
|
NM_000477.5:c.1437G>A
|
NP_000468.1:p.Val479=
|
|
NM_000477.6:c.1437G>A
|
NP_000468.1:p.Val479=
|
|
NM_000477.7:c.1437G>A
MANE Select
|
NP_000468.1:p.Val479=
|
|